Medical Device Recalls
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1 result found
510(K) Number: K982960 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Tru-Core II Disposable Automatic Biopsy Instrument and Tru-Core II URO Disposable Automatic Biopsy I... | 2 | 10/08/2010 |
FEI # 1036710 Medical Device Technologies, Inc. |
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